Camuzat A - Search Results

1

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.

Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A; French Dystonia Network. Clot F, et al. Among authors: camuzat a. Brain. 2009 Jul;132(Pt 7):1753-63. doi: 10.1093/brain/awp084. Epub 2009 Jun 2. Brain. 2009. PMID: 19491146

2

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Brassat D, Camuzat A, Vidailhet M, Feki I, Jedynak P, Klap P, Agid Y, Dürr A, Brice A. Brassat D, et al. Among authors: camuzat a. Arch Neurol. 2000 Mar;57(3):333-5. doi: 10.1001/archneur.57.3.333. Arch Neurol. 2000. PMID: 10714658

3

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation.

Herman-Bert A, Stevanin G, Netter JC, Rascol O, Brassat D, Calvas P, Camuzat A, Yuan Q, Schalling M, Dürr A, Brice A. Herman-Bert A, et al. Among authors: camuzat a. Am J Hum Genet. 2000 Jul;67(1):229-35. doi: 10.1086/302958. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820125 Free PMC article.

4

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Among authors: camuzat a. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

5

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

Fujigasaki H, Martin JJ, De Deyn PP, Camuzat A, Deffond D, Stevanin G, Dermaut B, Van Broeckhoven C, Dürr A, Brice A. Fujigasaki H, et al. Among authors: camuzat a. Brain. 2001 Oct;124(Pt 10):1939-47. doi: 10.1093/brain/124.10.1939. Brain. 2001. PMID: 11571212

6

Spinocerebellar ataxia type 10 in the French population.

Fujigasaki H, Tardieu S, Camuzat A, Stevanin G, LeGuern E, Matsuura T, Ashizawa T, Dürr A, Brice A. Fujigasaki H, et al. Among authors: camuzat a. Ann Neurol. 2002 Mar;51(3):408-9. doi: 10.1002/ana.10126. Ann Neurol. 2002. PMID: 11891842 No abstract available.

7

Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.

Caparros-Lefebvre D, Sergeant N, Lees A, Camuzat A, Daniel S, Lannuzel A, Brice A, Tolosa E, Delacourte A, Duyckaerts C. Caparros-Lefebvre D, et al. Among authors: camuzat a. Brain. 2002 Apr;125(Pt 4):801-11. doi: 10.1093/brain/awf086. Brain. 2002. PMID: 11912113

8

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Stevanin G, Camuzat A, Holmes SE, Julien C, Sahloul R, Dodé C, Hahn-Barma V, Ross CA, Margolis RL, Durr A, Brice A. Stevanin G, et al. Among authors: camuzat a. Neurology. 2002 Mar 26;58(6):965-7. doi: 10.1212/wnl.58.6.965. Neurology. 2002. PMID: 11914418

9

Association between the extended tau haplotype and frontotemporal dementia.

Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, Brice A. Verpillat P, et al. Among authors: camuzat a. Arch Neurol. 2002 Jun;59(6):935-9. doi: 10.1001/archneur.59.6.935. Arch Neurol. 2002. PMID: 12056929

10

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A. Stevanin G, et al. Among authors: camuzat a. Brain. 2003 Jul;126(Pt 7):1599-603. doi: 10.1093/brain/awg155. Epub 2003 May 6. Brain. 2003. PMID: 12805114

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